EP1652878A1 - Composition de caoutchouc et pneu la comprenant - Google Patents

Composition de caoutchouc et pneu la comprenant Download PDF

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Publication number
EP1652878A1
EP1652878A1 EP05020725A EP05020725A EP1652878A1 EP 1652878 A1 EP1652878 A1 EP 1652878A1 EP 05020725 A EP05020725 A EP 05020725A EP 05020725 A EP05020725 A EP 05020725A EP 1652878 A1 EP1652878 A1 EP 1652878A1
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EP
European Patent Office
Prior art keywords
weight
parts
amount
rubber
styrene
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Granted
Application number
EP05020725A
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German (de)
English (en)
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EP1652878B1 (fr
Inventor
Tetsuya Kunisawa
Toshiro Matsuo
Takuya Horiguchi
Takashi Nakamura
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Sumitomo Rubber Industries Ltd
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Sumitomo Rubber Industries Ltd
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Publication of EP1652878A1 publication Critical patent/EP1652878A1/fr
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Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L9/00—Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
    • C08L9/06—Copolymers with styrene
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L21/00—Compositions of unspecified rubbers
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00—Use of inorganic substances as compounding ingredients
    • C08K3/01—Use of inorganic substances as compounding ingredients characterized by their specific function
    • C08K3/013—Fillers, pigments or reinforcing additives
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/54—Silicon-containing compounds
    • C08K5/548—Silicon-containing compounds containing sulfur
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L45/00—Compositions of homopolymers or copolymers of compounds having no unsaturated aliphatic radicals in side chain, and having one or more carbon-to-carbon double bonds in a carbocyclic or in a heterocyclic ring system; Compositions of derivatives of such polymers
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L7/00—Compositions of natural rubber
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L9/00—Compositions of homopolymers or copolymers of conjugated diene hydrocarbons

Definitions

  • the present invention relates to a rubber composition and a tire comprising the same, and specifically, relates to a rubber composition which can prepare a tire having improved grip performance, grip durability and abrasion resistance.
  • a rubber composition for a tire containing a liquid polymer having a specific molecular weight is described in Japanese Unexamined Patent Publication JP-A-No. 06-200075, but the rubber composition could not improve the grip performance, grip durability and abrasion resistance with a good balance.
  • the present invention relates to a rubber composition
  • a rubber composition comprising:
  • the above-described rubber composition further contains preferably 2 to 12 parts by weight of a silane coupling agent represented by the following formula: (C n H 2n+1 O) 3 -Si-(CH 2 ) m -S 1 (CH 2 ) m -Si-(C n H 2n+1 O) 3 (wherein n is an integer of 1 to 3, m is an integer of 1 to 4 and the average value of 1 is 1.8 to 3.5), based on 100 parts by weight of the above-described silica and is obtained by kneading at condition of at least 150°C.
  • a silane coupling agent represented by the following formula: (C n H 2n+1 O) 3 -Si-(CH 2 ) m -S 1 (CH 2 ) m -Si-(C n H 2n+1 O) 3 (wherein n is an integer of 1 to 3, m is an integer of 1 to 4 and the average value of 1 is 1.8 to 3.5), based on 100
  • the present invention relates to a tire having tread comprising the above-described rubber composition.
  • the rubber composition of the present invention comprises a diene rubber, a reinforcing filler, a styrene-butadiene polymer and an indene resin.
  • the diene rubber comprises a solution-polymerized styrene-butadiene rubber (S-SBR) and a natural rubber (NR) and/or a butadiene rubber (BR).
  • S-SBR solution-polymerized styrene-butadiene rubber
  • NR natural rubber
  • BR butadiene rubber
  • S-SBR is obtained by solution polymerization.
  • SBR those which is obtained by emulsion polymerization (an emulsion polymerization SBR) are also known, but the emulsion-polymerized SBR contains an emulsifier and it is disadvantageous to grip decrease (phenomenon in which steering stability is deteriorated since a tire rubber generates heat by running). Further, since S-SBR is inferior in low fuel consumption to the solution-polymerized SBR, SBR obtained by solution polymerization is used.
  • Weight average molecular weight (Mw) of S-SBR is at least 500,000 and preferably at least 600,000. When Mw is less than 500,000, it is not preferable since abrasion resistance is deteriorated. Further, Mw is at most 2,500,000, preferably at most 2,000,000 and more preferably at most 1,500,000. When Mw is more than 2,500,000, processability is remarkably deteriorated in a process of kneading and, also, since S-SBR has a high molecular weight, preparations by current polymer preparation techniques are difficult; therefore, S-SBR tends to be at a high cost.
  • S-SBR those which are made to have a high molecular weight by coupling with tin or silicon are preferable.
  • An example of the coupling process is a process of reacting an alkali metal (such as Li) or an alkali earth metal (such as Mg) at the terminal of S-SBR molecular chain with tin halide or silicon halide, according to conventional processes.
  • the amount of styrene of S-SBR is at least 20 % by weight and preferably at least 25 % by weight. When the amount of styrene is less than 20 % by weight, grip performance is lowered. Further, the amount of styrene is at most 40 % by weight. When the amount of styrene is more than 40 % by weight, a rubber becomes hard at a tire running at a low temperature and the lowering of the grip performance is caused.
  • the amount of styrene is obtained by measuring 1 H NMR by using an NMR device and calculating from phenyl proton based on a styrene unit at 6.7 to 7.2 ppm which was determined from the spectrum of the obtained S-SBR.
  • the amount of vinyl of S-SBR (the part of butadiene) is at least 30 % by weight and preferably at least 35 % by weight. When the amount of vinyl is less than 30 % by weight, it is not preferable since grip performance is lowered. Further, the amount of vinyl is at most 60 % by weight and preferably at most 55 % by weight. When the amount of vinyl is more than 60 % by weight, low fuel consumption is not achieved.
  • the amount of vinyl is obtained by measuring 1 H NMR by using an NMR device and calculating from the methylene proton of a vinyl bond based on a butadiene unit at 4.7 to 5.2 ppm which is determined from the spectrum of the obtained S-SBR.
  • the amount of S-SBR is at least 60 % by weight in the diene rubber and preferably at least 70 % by weight. When the amount is less than 60 % by weight, it is not preferable since grip performance is lowered. Also, the amount of S-SBR is more preferably at most 95 % by weight. When the amount is more than 95 % by weight, the rubber becomes hard at tire running at a low temperature and grip performance tends to be lowered.
  • the amount of NR and/or BR is preferably at least 5 % by weight in the diene rubber and more preferably at least 10 % by weight. When the amount is less than 5 % by weight, a brittleness temperature becomes high and a rubber tends to be cracked at using in extreme cold. Also, the amount of NR and/or BR is at most 40 % by weight in the diene rubber and preferably at most 35 % by weight. When the amount is more than 40 % by weight, it is not preferable since grip is lowered.
  • a polyisoprene rubber (IR), an ethylene-propylene-diene rubber (EPDM), a chloroprene rubber (CR), an acrylonitrile-butadiene rubber (NBR), a butyl rubber (IIR) and the like can be also used other than the above-described S-SBR, BR and NR.
  • the reinforcing filler comprises carbon black and silica.
  • the nitrogen adsorbing-specific surface area (N 2 SA) of carbon black is at least 100 m 2 /g and preferably at least 110 m 2 /g.
  • N 2 SA is at most 250 m 2 /g and preferably at most 240 m 2 /g.
  • N 2 SA is more than 250 m 2 /g, low fuel consumption tends not to be achieved.
  • the iodine adsorption amount (IA) of carbon black is at least 110 mg/g and preferably at least 115 mg/g. When IA is less than 110 mg/g, abrasion resistance and grip performance are lowered. Also, IA is at most 200 mg/g and preferably at most 195 mg/g. When IA is more than 200 mg/g, low fuel consumption can not be achieved and processability is deteriorated.
  • Cetyltrimethylammonium bromide (CTAB) adsorbing-specific surface area of carbon black is preferably 94 to 240 ml/100g.
  • CTAB adsorbing specific surface area is less than 94 ml/100g, abrasion resistance and grip performance tend to be lowered and when it is more than 240 ml/ 100g, low fuel consumption can not be achieved and processability tends to be deteriorated.
  • CTAB/IA cetyltrimethylammonium bromide
  • IA iodine adsorption amount
  • the amount of carbon black is preferably at least 20 parts by weight based on 100 parts by weight of the above-described diene rubber and more preferably at least 25 parts by weigh. When the amount is less than 20 parts by weight, grip performance and abrasion resistance on a dry road surface tend to be lowered. Also, the amount of carbon black is preferably at most 100 parts by weight and more preferably at most 95 parts by weigh. When the amount is more than 100 parts by weight, viscosity of the rubber is raised and processability tends to be deteriorated.
  • silica there is not a particular limitation, and those which are prepared by a wet process or a dry process can be used.
  • the amount of silica is at least 10 parts by weight based on 100 parts by weight of the above-described diene rubber, preferably at least 15 parts by weight and more preferably at least 25 parts by weight. When the amount is less than 10 parts by weight, grip performance becomes inferior. Also, the amount of silica is at most 100 parts by weight and preferably at most 95 parts by weight. When the amount is more than 100 parts by weight, viscosity of the rubber is raised; thus, processability is deteriorated.
  • the amount of the reinforcing filler is at least 50 parts by weight based on 100 parts by weight of the above-described diene rubber and preferably at least 55 parts by weight. When the mount is less than 50 parts by weight, it is not preferable since abrasion resistance and grip performance are low. Further, the amount of the reinforcing filler is at most 120 parts by weight and preferably at most 115 parts by weight. When the amount is more than 120 parts by weight, low fuel consumption can not be achieved.
  • reinforcing filler along with those except for the above-described carbon black and silica, calcium carbonate, clay and the like can be used.
  • the rubber composition of the present invention can use a combination of a silane coupling agent with silica.
  • a reaction temperature in a kneader is highly set to carry out the reaction of silica with the diene rubber efficiently.
  • the temperature is set at least 150°C and, in particular, 160 to 180°C.
  • the reaction temperature is less than 150°C, the reaction of silica with a silane coupling agent tends to be hardly completed, and when the temperature is more than 180°C, viscosity of the rubber at kneading tends to be excessively raised.
  • the silane coupling agent represented by the following formula: (C n H 2n+1 O) 3 -Si-(CH 2 )m-Si-(CH 2 )m-Si-(C n H 2n+1 O) 3 (wherein n is an integer of 1 to 3, m is an integer of 1 to 4 and the average value of 1 is 1.8 to 3.5), can be used as the silane coupling agent for silica in place of a conventional Si69 (four sulfur atoms in one molecule) and the like.
  • An example of silane coupling agent satisfying the formula is Si266 (contains two sulfur atoms in one molecule, high purity) and the like.
  • silane coupling agent 2 to 12 parts by weight of the silane coupling agent based on 100 parts by weight of silica.
  • amount of silane coupling agent is less than 2 parts by weight, performance of silica can not be brought out sufficiently and wet grip performance and abrasion resistance tend to be inferior, and when the amount of the silane coupling agent is more than 12 parts by weight, the silane coupling agent is excessive and costs high, and abrasion resistance tends to be inferior.
  • the rubber composition of the present invention uses a styrene-butadiene polymer as a softening agent.
  • a styrene-butadiene polymer as a softening agent.
  • diene polymers such as an isoprene polymer and a butadiene polymer other than the styrene-butadiene polymer, but when these are used, a disadvantage of which the grip performance is lowered is occurred; therefore, the styrene-butadiene polymer is used in the present invention.
  • Weight average molecular weight (Mw) of the styrene-butadiene polymer is at least 1,000 and preferably at least 1,500. When Mw is less than 1,000, it is risky since the styrene-butadiene polymer blooms out on the surface of the rubber. Also, Mw of the styrene-butadiene polymer is at most 15,000, preferably at most 13,000 and more preferably at most 10,000. When Mw is more than 15,000, viscosity of the rubber increases and processability is deteriorated.
  • the amount of styrene of the styrene-butadiene polymer is at least 17 % by weight and preferably at least 19 % by weight. When the amount of styrene is less than 17 % by weight, lowering of grip tends to be caused. Also, the amount of styrene of the styrene-butadiene polymer is at most 27 % by weight and preferably at most 25 % by weight. When the amount of styrene is more than 27 % by weight, viscosity of the rubber increase and processability tends to be deteriorated.
  • the amount of vinyl of the styrene-butadiene polymer is at least 60 % by weight and preferably at least 65 % by weight. When the amount of vinyl is less than 60 % by weight, grip tends to be lowered. Also, the amount of vinyl of the styrene-butadiene polymer is at most 80 % by weight and preferably at most 75 % by weight. When the amount of vinyl is more than 80 % by weight, it is not preferable since grip and a crosslinking density tend to decrease and the rubber becomes soft.
  • the amount of the styrene-butadiene polymer is at least 2 parts by weight based on 100 parts by weight of the diene rubber and preferably at least 3 parts by weight. When the amount is less than 2 parts by weight, improvement in grip cannot be expected. Also, the amount of the styrene-butadiene polymer is at most 50 parts by weight based on 100 parts by weight of the diene rubber, preferably at most 45 parts by weight and more preferably at most 40 parts by weight. When the amount is more than 50 parts by weight, the rubber becomes excessively soft; therefore, steering stability and abrasion resistance tend to be deteriorated.
  • indene resin is specifically a coumarone indene resin and, among these, since the grip performance becomes high, it is preferable to use the coumarone indene resin.
  • a tackifier resin examples such as an aromatic petroleum resin (a resin of C9 distillate), a terpene resin, an aromatic modified terpene resin, a rosin resin, a phenol resin, a petroleum resin (a resin of C5 distillate) other than indene resins are generally used, but since disadvantage of which the grip performance and grip durability cannot be improved in a good balance by using the tackifier resin except for the indene resin in the present invention is occurred, the indene resins are used in the present invention.
  • the meting point of the indene resin is at least 100°C and preferably at least 110°C. When the meting point is less than 100°C, the rubber becomes excessively soft during running; therefore, steering stability tends to be deteriorated.
  • the meting point of the indene resin is at most 150°C and preferably at most 140°C. When the meting point is more than 150°C, there is fear of deterioration of processability by increasing the viscosity of the rubber.
  • the amount of the indene resin is at least 2 parts by weight based on 100 parts by weight of the diene rubber and preferably at least 3 parts by weight. When the amount is less than 2 parts by weight, abrasion resistance, dry grip and grip durability are not improved. Also, the amount of the indene resin is at most 25 parts by weight based on 100 parts by weight of the diene rubber and preferably at most 23 parts by weight. When the amount is more than 25 parts by weight, it is not preferable since the abrasion resistance tends to be deteriorated.
  • the rubber composition of the present invention can contain a softening agent such as an oil, a vulcanizing agent such as sulfur, an antioxidant, wax, stearic acid, zinc oxide and a vulcanization accelerator other than the above-described diene rubber, the reinforcing filler, the silane coupling agent, the styrene-butadiene polymer and the indene resin.
  • a softening agent such as an oil
  • a vulcanizing agent such as sulfur, an antioxidant, wax, stearic acid, zinc oxide and a vulcanization accelerator other than the above-described diene rubber
  • the reinforcing filler such as silane coupling agent, the styrene-butadiene polymer and the indene resin.
  • the rubber composition of the present invention is prepared by a general process. Namely, after kneading the above-described compounding agents and an additive, if necessary, with a banbury mixer, an open roll and the like, the rubber composition can be prepared by vulcanizing the mixture.
  • the toluene swelling rate of the rubber composition of the present invention is preferably at least 180 % and more preferably at least 220 %.
  • the toluene swelling rate is preferably at most 320 % and more preferably at most 310 %.
  • the toluene swelling rate is obtained by immersing a rubber cube in which one side is adjusted at about 5 mm in toluene for 24 hours and, then, measuring weight ratios before immersion and after immersion.
  • the tire of the present invention has tread comprising the above-described rubber composition.
  • the tire of the present invention is prepared by a general process in tire industries. Namely, after kneading as mentioned above, the obtained kneaded product is molded in a shape of a tread on a tire molding machine, and laminated with other tire parts and, then, the tire of the present invention can be prepared by vulcanization.
  • SBR T4350 available from ASAHI KASEI CORP. (weight average molecular weight: 600,000 to 1,000,000, amount of styrene: 39 % by weight, amount of vinyl: 38 % by weight, amount of an oil: 33.3 % by weight)
  • BR BR available from Ube Industries, Ltd.
  • Silica ULTRASIL VN3 available from Degussa Co.
  • Silane coupling agent Si266 (bis (3-triethoxysilylpropyl) disulfide) (average value of 1 in the formula: 2.2) available from Degussa Co. (C 2 H 5 O) 3 -Si-(CH 2 ) 3 -Si-(CH 2 ) 3 -Si-(OC 2 H 5 ) 3
  • Process oil Diana Process PS 32 available from Idemitsu Kosan Co., Ltd.
  • Wax SUNNOC Wax available from Ouchi Shinko Chemical Industrial Co., Ltd.
  • Antioxidant SANTOFLEX 13 available from FLEXSYS Co.
  • Stearic acid Poulownia (KIRI) available from NOF Corporation
  • Zinc flower ZINC OXIDE NO.2 available from Mitsui Mining And Smelting Co., Ltd.
  • Styrene-butadiene polymer Ricon 100 (weight average molecular weight: 4,000 to 5,000, amount of styrene: 20 % by weight, amount of vinyl: 70 % by weight) available from Sartomer Company Inc.
  • Resin ESCURON V120 (a coumarone indene resin, a melting point: 120°C) available from Nippon Steel Chemical Co., Ltd.
  • Sulfur Sulfur powder available from Tsurumi Chemicals Co., Ltd.
  • Vulcanization accelerator 1 NOCCELER NS available from Ouchi Shinko Chemical Industrial Co., Ltd.
  • Vulcanization accelerator 2 SOXINOL D available from Sumitomo Chemical Co., Ltd.
  • composition contents in Table 1 excluding sulfur and a vulcanization accelerator were kneaded at 165°C using a 1.7 L banbury mixer made by Kobe Steel, Ltd., sulfur and a vulcanization accelerator were added to the obtained kneaded products, and the mixture kneaded at 110°C with a twin roller was vulcanized at 175°C for 10 min to prepare the rubber compositions.
  • Abrasion quantity was measured from the prepared rubber composition under conditions of a room temperature, a loading weight of 2.0 kgf and a slip rate of 30 % by using a lambourn abrasion tester.
  • the reciprocal number of the abrasion quantity was represented as an index, regarding Comparative Example as 100. The larger the value is, the higher abrasion resistance is.
  • Tires with a size of 215/40R17 having a tread comprising the above-described rubber composition were prepared. Measurement below was conducted using a vehicle loaded with the tires.
  • Abrasion resistance, dry grip and grip durability are improved with a highly good balance in Examples 1 to 3, in which a combination of Ricon 100 and V120 in an appropriate amounts are used.
  • Comparative Example 3 in which only V120 is used, although the dry grip is improved, abrasion resistance and grip durability are slightly lowered.
  • Abrasion resistance is slightly deteriorated in Comparative Example 4, in which a combination of Ricon 100 and V120 are used excessively in the range of the appropriate amount.
  • the grip performance, the grip durability and abrasion resistance of a tire in which the rubber composition is used as a tread can be improved with a good balance by compounding specific amounts of a particular styrene-butadiene polymer and an indene resin with a rubber composition containing a diene rubber and a reinforcing filler.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Tires In General (AREA)
EP05020725A 2004-11-01 2005-09-22 Composition de caoutchouc et pneu la comprenant Ceased EP1652878B1 (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2004317972A JP4138729B2 (ja) 2004-11-01 2004-11-01 ゴム組成物およびそれからなるタイヤ

Publications (2)

Publication Number Publication Date
EP1652878A1 true EP1652878A1 (fr) 2006-05-03
EP1652878B1 EP1652878B1 (fr) 2011-02-23

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EP05020725A Ceased EP1652878B1 (fr) 2004-11-01 2005-09-22 Composition de caoutchouc et pneu la comprenant

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US (1) US7829621B2 (fr)
EP (1) EP1652878B1 (fr)
JP (1) JP4138729B2 (fr)
CN (1) CN100352851C (fr)
DE (1) DE602005026487D1 (fr)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1690895A1 (fr) * 2005-02-10 2006-08-16 Sumitomo Rubber Industries, Ltd. Composition de caoutchouc et pneumatique comprenant bande de roulement comprenant celle-ci
EP2103650A1 (fr) * 2007-01-11 2009-09-23 Bridgestone Corporation Composition de caoutchouc et pneu utilisant celle-ci
ITTO20100476A1 (it) * 2010-06-07 2011-12-08 Bridgestone Corp Mescola per battistrada per pneumatici invernali
US20120157568A1 (en) * 2010-12-21 2012-06-21 Paul Harry Sandstrom Silica reinforced rubber composition with combination of functionalized elastomer, liquid polymer and resin and tire with tread thereof
EP3214111A4 (fr) * 2014-10-27 2017-09-06 Bridgestone Corporation Procédé de production d'une composition de caoutchouc, composition de caoutchouc et pneu
US10160847B2 (en) 2010-11-26 2018-12-25 Compagnie Generale Des Etablissments Michelin Tyre tread
US10843508B2 (en) 2017-02-13 2020-11-24 Cooper Tire & Rubber Company Guayule tire tread compound
CN112004880A (zh) * 2018-08-06 2020-11-27 住友橡胶工业株式会社 充气轮胎

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JP2007332246A (ja) * 2006-06-14 2007-12-27 Bridgestone Corp ゴム組成物及びそれを用いたタイヤ
KR100782969B1 (ko) 2006-12-20 2007-12-07 한국타이어 주식회사 승용차용 타이어 트레드 고무 조성물
JP2008163129A (ja) * 2006-12-27 2008-07-17 Yokohama Rubber Co Ltd:The タイヤトレッド用ゴム組成物
KR101132791B1 (ko) * 2009-12-21 2012-04-02 한국타이어 주식회사 타이어 트레드용 고무 조성물 및 이를 이용하여 제조한 타이어
JP4835769B2 (ja) * 2010-05-26 2011-12-14 横浜ゴム株式会社 タイヤトレッド用ゴム組成物
CN102336939B (zh) * 2010-07-16 2014-10-22 住友橡胶工业株式会社 用于胎面的橡胶组合物和充气轮胎
FR2968307B1 (fr) * 2010-11-26 2018-04-06 Societe De Technologie Michelin Bande de roulement de pneumatique
CN102532627A (zh) * 2010-12-06 2012-07-04 固特异轮胎和橡胶公司 充气轮胎
US9126457B2 (en) 2010-12-06 2015-09-08 The Goodyear Tire & Rubber Company Pneumatic tire having first tread cap zone and second tread cap zone
JP5351244B2 (ja) * 2011-04-22 2013-11-27 住友ゴム工業株式会社 タイヤ用ゴム組成物、及び空気入りタイヤ
BR112014001823A2 (pt) 2011-07-28 2017-02-21 Sumitomo Rubber Ind pneumático
JP5559234B2 (ja) 2011-08-09 2014-07-23 住友ゴム工業株式会社 タイヤ用ゴム組成物及び空気入りタイヤ
JP5668660B2 (ja) * 2011-09-30 2015-02-12 横浜ゴム株式会社 タイヤ用ゴム組成物及びこれを用いる空気入りタイヤ
JP5443554B2 (ja) 2012-08-01 2014-03-19 住友ゴム工業株式会社 インナーライナーを備えた空気入りタイヤ
JP5342684B1 (ja) * 2012-09-11 2013-11-13 住友ゴム工業株式会社 インナーライナーを備えた空気入りタイヤ
CN102838786B (zh) * 2012-09-20 2015-12-16 北京彤程创展科技有限公司 一种橡胶组合物、以及使用该组合物的轮胎胎面及轮胎
US20140256858A1 (en) 2013-03-11 2014-09-11 Robert Anthony Bethea Solution polymerization prepared styrene/butadiene elastomer containing liquid styrene/butadiene polymer and tire with component
US10280278B2 (en) * 2013-05-24 2019-05-07 Bridgestone Corporation Rubber composition
JP6115319B2 (ja) * 2013-05-28 2017-04-19 横浜ゴム株式会社 タイヤ用ゴム組成物および空気入りタイヤ
JP6733223B2 (ja) * 2016-03-07 2020-07-29 住友ゴム工業株式会社 高性能タイヤ
CN105623018B (zh) * 2016-03-22 2018-05-15 中策橡胶集团有限公司 一种超低滚动阻力轮胎胎面胶料及其炼胶方法和轮胎
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WO2018097066A1 (fr) * 2016-11-24 2018-05-31 住友ゴム工業株式会社 Composition de caoutchouc pour bande de roulement, et pneu
JP7081082B2 (ja) * 2017-03-17 2022-06-07 住友ゴム工業株式会社 タイヤ用ゴム組成物及び空気入りタイヤ
JP7013674B2 (ja) * 2017-04-19 2022-02-01 住友ゴム工業株式会社 タイヤ
US10570275B2 (en) 2017-08-30 2020-02-25 The Goodyear Tire & Rubber Company Pneumatic tire having tread with alkoxysilane-terminated polybutadiene
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JP7529960B2 (ja) * 2019-09-06 2024-08-07 横浜ゴム株式会社 タイヤ用ゴム組成物およびそれを用いた空気入りタイヤ

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EP1690895A1 (fr) * 2005-02-10 2006-08-16 Sumitomo Rubber Industries, Ltd. Composition de caoutchouc et pneumatique comprenant bande de roulement comprenant celle-ci
EP2103650A1 (fr) * 2007-01-11 2009-09-23 Bridgestone Corporation Composition de caoutchouc et pneu utilisant celle-ci
EP2103650A4 (fr) * 2007-01-11 2010-02-17 Bridgestone Corp Composition de caoutchouc et pneu utilisant celle-ci
US8318861B2 (en) 2007-01-11 2012-11-27 Bridgestone Corporation Rubber composition and tire using the same
ITTO20100476A1 (it) * 2010-06-07 2011-12-08 Bridgestone Corp Mescola per battistrada per pneumatici invernali
US10160847B2 (en) 2010-11-26 2018-12-25 Compagnie Generale Des Etablissments Michelin Tyre tread
US20120157568A1 (en) * 2010-12-21 2012-06-21 Paul Harry Sandstrom Silica reinforced rubber composition with combination of functionalized elastomer, liquid polymer and resin and tire with tread thereof
EP3214111A4 (fr) * 2014-10-27 2017-09-06 Bridgestone Corporation Procédé de production d'une composition de caoutchouc, composition de caoutchouc et pneu
US10843508B2 (en) 2017-02-13 2020-11-24 Cooper Tire & Rubber Company Guayule tire tread compound
US11465446B2 (en) 2017-02-13 2022-10-11 Cooper Tire & Rubber Company Natural rubber tire tread compound
CN112004880A (zh) * 2018-08-06 2020-11-27 住友橡胶工业株式会社 充气轮胎
EP3747943A4 (fr) * 2018-08-06 2021-06-09 Sumitomo Rubber Industries, Ltd. Pneumatique
US12091550B2 (en) 2018-08-06 2024-09-17 Sumitomo Rubber Industries, Ltd. Pneumatic tire

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JP4138729B2 (ja) 2008-08-27
CN1769331A (zh) 2006-05-10
DE602005026487D1 (de) 2011-04-07
JP2006124601A (ja) 2006-05-18
US7829621B2 (en) 2010-11-09
EP1652878B1 (fr) 2011-02-23
US20060094815A1 (en) 2006-05-04

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